# Rectovaginal Fistula in a 10-Year-Old With Hirschsprung Disease: A Case Report

**Authors:** Jomaries O Gomez Rosado, Courteney Castellano, Jossias Genao Cruz, Jonas Esgusquiza

PMC · DOI: 10.7759/cureus.57316 · Cureus · 2024-03-31

## TL;DR

A 10-year-old girl with Hirschsprung disease developed a rare rectovaginal fistula after complications following a colectomy.

## Contribution

This report highlights a rare complication of Hirschsprung disease in a pediatric patient.

## Key findings

- A 10-year-old with Hirschsprung disease developed a rectovaginal fistula.
- The patient had multiple colonic ulcers, severe anemia, and fecal incontinence.
- This case emphasizes the need for awareness of rare complications in Hirschsprung disease.

## Abstract

Hirschsprung disease is an uncommon medical condition caused by the lack of migration of ganglion cells to the rectum during embryonic development, affecting the peristaltic movements of the intestine. It is a chronic medical condition responsible for chronic constipation and intestinal obstruction. We present the case of a 10-year-old female with a history of Hirschsprung disease and colectomy admitted to a pediatric hospital for the management of multiple colonic ulcers and severe anemia who subsequently developed a rectovaginal fistula. This patient's admission was complicated by perianal and vaginal excoriations, a paralytic ileus, and fecal incontinence. This case report is unique due to the development of a rare pediatric complication of Hirschsprung disease.

## Linked entities

- **Diseases:** Hirschsprung disease (MONDO:0007723), paralytic ileus (MONDO:0004568)

## Full-text entities

- **Diseases:** fecal incontinence (MESH:D005242), Rectovaginal Fistula (MESH:D012006), constipation (MESH:D003248), colonic ulcers (MESH:D003108), anemia (MESH:D000740), intestinal obstruction (MESH:D007415), paralytic ileus (MESH:D007418), Hirschsprung Disease (MESH:D006627)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC11060009/full.md

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Source: https://tomesphere.com/paper/PMC11060009